A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14026619



Internal ID21175436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111631320..111631320hg38UCSC Ensembl
chr13:112283667..112283667hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3057082
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
AnalysisCombines the NGS (e.g., Illumina) and SMS (e.g., Pacbio) for detecting large and small SVs (parameters the same as commit eee31f6 of https://bitbucket.org/xianfan/hybridassemblysv)
Platform
Comments
ReferenceFan_et_al_2017
Pubmed ID28104618
Accession Number(s)nssv14026619
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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